Vinylogous aldol reaction: a valuable, yet understated carbon-carbon bond-forming maneuver

Giovanni Casiraghi; Franca Zanardi; Giovanni Appendino; Gloria Rassu

doi:10.1021/cr990247i

Vinylogous aldol reaction: a valuable, yet understated carbon-carbon bond-forming maneuver

Giovanni Casiraghi
, Franca Zanardi
, Giovanni Appendino
, Gloria Rassu

Research output: Contribution to journal › Article › peer-review

Abstract

The vinylogous aldol reactions provides access to a range of structurally diverse targets but has long remained a marginally explored area of organic synthesis. However, its applications have burgeoned in the past few years. Examples are given to demonstrate that vinylogous dienolates and their synthons have a sumptuos aldol chemistry.

Original language	English
Pages (from-to)	1929-1972
Number of pages	44
Journal	Chemical Reviews
Volume	100
Issue number	6
DOIs	https://doi.org/10.1021/cr990247i
Publication status	Published - Jun 2000
Externally published	Yes

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title = "Vinylogous aldol reaction: a valuable, yet understated carbon-carbon bond-forming maneuver",

abstract = "The vinylogous aldol reactions provides access to a range of structurally diverse targets but has long remained a marginally explored area of organic synthesis. However, its applications have burgeoned in the past few years. Examples are given to demonstrate that vinylogous dienolates and their synthons have a sumptuos aldol chemistry.",

author = "Giovanni Casiraghi and Franca Zanardi and Giovanni Appendino and Gloria Rassu",

year = "2000",

month = jun,

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AU - Casiraghi, Giovanni

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AU - Appendino, Giovanni

AU - Rassu, Gloria

PY - 2000/6

Y1 - 2000/6

N2 - The vinylogous aldol reactions provides access to a range of structurally diverse targets but has long remained a marginally explored area of organic synthesis. However, its applications have burgeoned in the past few years. Examples are given to demonstrate that vinylogous dienolates and their synthons have a sumptuos aldol chemistry.

AB - The vinylogous aldol reactions provides access to a range of structurally diverse targets but has long remained a marginally explored area of organic synthesis. However, its applications have burgeoned in the past few years. Examples are given to demonstrate that vinylogous dienolates and their synthons have a sumptuos aldol chemistry.

UR - https://www.scopus.com/pages/publications/0033690703

U2 - 10.1021/cr990247i

DO - 10.1021/cr990247i

M3 - Article

SN - 0009-2665

VL - 100

SP - 1929

EP - 1972

JO - Chemical Reviews

JF - Chemical Reviews

IS - 6

ER -

Vinylogous aldol reaction: a valuable, yet understated carbon-carbon bond-forming maneuver

Abstract

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